Evidence map›Paper›PMID 31342675›Full record

ArticleMolecular genetics & genomic medicine2019

Impact of CHRNA5 polymorphisms on the risk of schizophrenia in the Chinese Han population.

Dafei Zhan, Qiankun Yao, Shaojian Fu, Xianglai Liu, Jun Zhou, Daqiang Chen, Chuanlong Yu

Open access · goldAbstract read
In one paragraph

Article in Molecular genetics & genomic medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.1field-weighted citation impact, top 54% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 3 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Dafei ZhanDivision of Prevention, Hainan Provincial Anning Hospital, Haikou, China.
Qiankun YaoDivision of Prevention, Hainan Provincial Anning Hospital, Haikou, China.ORCID 0000-0001-8324-9773
Shaojian FuDivision of Prevention, Hainan Provincial Anning Hospital, Haikou, China.
Xianglai LiuDivision of Prevention, Hainan Provincial Anning Hospital, Haikou, China.
Jun ZhouDivision of Prevention, Hainan Provincial Anning Hospital, Haikou, China.
Daqiang ChenDivision of Prevention, Hainan Provincial Anning Hospital, Haikou, China.
Chuanlong YuDivision of Prevention, Hainan Provincial Anning Hospital, Haikou, China.
Hainan Center for Disease Control & Prevention · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSchizophrenia is a complex mental disease whose cause is still unknown. Neuronal nicotinic acetylcholine receptors (nAChRs) have been implicated in various neurological disorders, including schizophrenia. The previous reports have shown that CHRNA polymorphisms were involved in schizophrenia. This study is to explore the potential association between CHRNA5 (OMIM#118505) polymorphisms and schizophrenia susceptibility in a Chinese population. METHODS AND

resultsA case-control study was conducted with 384 schizophrenia patients and 687 controls. We genotyped eight single nucleotide polymorphisms (SNPs) distributed in CHRNA5. Regulome DB, HaploReg, and GTEx databases were used to calculate possible functional effects of the polymorphisms. The χ

conclusionsOverall, our findings supported that the potential association existed between CHRNA5 polymorphisms and schizophrenia susceptibility in a Chinese population. But, large sample validation is needed to enhance the accuracy of our results.

Indexed as

Genetic Predisposition to DiseasePolymorphism, Single NucleotideAdultAllelesBiomarkersCase-Control StudiesChinaFemaleGenetic Association StudiesGenotypeHaplotypesHumansLinkage DisequilibriumMaleMiddle AgedNerve Tissue ProteinsBiomarkersCHRNA5 protein, humanNerve Tissue ProteinsReceptors, NicotinicCHRNA5Neuronal nicotinic acetylcholine receptorsSchizophreniaSingle nucleotide polymorphism

Identifiers

PMID31342675
PMCPMC6732284
OpenAlexW2963397167

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.